Cannabidiol

CHEMBL190461 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
314.5 g/mol
LogP
6.5
Phase
4

A non-psychoactive cannabinoid derived from the cannabis plant, approved in purified oral form for treating seizures associated with Lennox-Gastaut syndrome and Dravet syndrome. It is thought to exert anticonvulsant effects through several mechanisms, including modulation of ion channels and inhibition of endocannabinoid reuptake. It is also widely used as an unregulated supplement for anxiety, pain, and sleep, though clinical evidence varies.

分子量

314.5000 g/mol

LogP

6.50

TPSA

40.50 Ų

リピンスキーの五則

適合

治療領域

作用機序

Modulates neuronal excitability through one or more mechanisms including blockade of voltage-gated sodium channels, enhancement of GABAergic inhibition, or modulation of calcium channels. This reduces the frequency and severity of seizure activity.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

Modulates neuronal excitability through one or more mechanisms including blockade of voltage-gated sodium channels, enhancement of GABAergic inhibition, or modulation of calcium channels. This reduces the frequency and severity of …

2D構造

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SMILES

C=C(C)[C@@H]1CCC(C)=C[C@H]1c1c(O)cc(CCCCC)cc1O

InChI

InChI=1S/C21H30O2/c1-5-6-7-8-16-12-19(22)21(20(23)13-16)18-11-15(4)9-10-17(18)14(2)3/h11-13,17-18,22-23H,2,5-10H2,1,3-4H3/t17-,18+/m0/s1

Molecular Formula

C21H30O2

HBD / HBA

2 / 2

回転可能結合数

6

重原子数

23

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

よくある質問

A non-psychoactive cannabinoid derived from the cannabis plant, approved in purified oral form for treating seizures associated with Lennox-Gastaut syndrome and Dravet syndrome. It is thought to exert anticonvulsant effects through several mechanisms, including modulation of ion channels and inhibition of endocannabinoid reuptake. It is also widely used as an unregulated supplement for anxiety, pain, and sleep, though clinical evidence varies.

Modulates neuronal excitability through one or more mechanisms including blockade of voltage-gated sodium channels, enhancement of GABAergic inhibition, or modulation of calcium channels. This reduces the frequency and severity of seizure activity.

Yes, Cannabidiol is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL190461. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 644019. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

医学的免責事項

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.